Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs361072 0.882 0.120 3 138759702 intron variant G/A;C snv 4
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4588
GC
0.597 0.720 4 71752606 missense variant G/A;T snv 1.6E-05; 0.25 53
rs4918 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs553668 0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs561017686 0.882 0.120 2 181678138 missense variant G/A;C snv 8.0E-06; 8.4E-04 4
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs7211 0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs777659543 0.882 0.120 11 74006231 missense variant G/A snv 4.0E-06 6
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7968585 0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1269801977 0.925 0.120 2 169604087 missense variant A/G snv 4.0E-06 7.0E-06 4
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs757431022 0.925 0.120 10 95432529 missense variant G/A snv 1.4E-04 4.2E-05 3
rs150016118 0.882 0.120 11 74006339 missense variant A/G snv 1.7E-05 6.3E-05 6